• PMID: 7686336
• Gene Name: CFTR
• Condition: congenital bilateral aplasia of the vas deferens
• Association: Compound heterozygosity for the delta F508 and F508C cystic fibrosis transmembrane conductance regulator(CFTR) mutations in a patient with congenital bilateral aplasia of the vas deferens.
• Mutation: delta F508 and F508C
• Population size: 1
• Population details: 1 congenital bilateral aplasia of the vas deferens
• Sex: Male
• Infertility type: Male infertility
• Other associated phenotypes: congenital bilateral aplasia of the vas deferens

Compound heterozygosity for the delta F508 and F508C cystic fibrosis transmembrane conductance regulator (CFTR) mutations in a patient with congenital bilateral aplasia of the vas deferens

Meschede D, Eigel A, Horst J, Nieschlag E.

No abstract available